Allele Registry

Canonical Allele Identifier: PA113557

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV000001324

RCV000274058

RCV000343151

RCV001293274

RCV001813931

RCV003125824

RCV003415614

RCV004018532

ClinVar Variation:

1262

HGVS (amino-acid)	Matching Registered Transcripts
NP_078846.2:p.Ala177Thr	CA251724 NM_024570.4:c.529G>A